Mahmoud Alsharbini
About Mahmoud Alsharbini
Mahmoud Alsharbini is an experienced EU MDR Quality Engineer with a strong background in healthcare quality and R&D, currently working at Redbock - an NES Fircroft company. He has held various roles in the medical device industry, demonstrating expertise in quality engineering and project management.
Current Role at Redbock - an NES Fircroft company
Mahmoud Alsharbini currently holds the position of EU MDR Quality Engineer at Redbock, which is part of NES Fircroft. He has been in this role since 2021. His responsibilities include ensuring compliance with EU Medical Device Regulation (MDR) standards, which is critical for the healthcare and medical device industries.
Previous Experience in Quality Engineering
Mahmoud has extensive experience in quality engineering across several organizations. He worked as a Quality Engineer III at Medline Industries, Inc. from 2017 to 2020. Prior to that, he served as a Quality Engineer at Midmark Corporation from 2014 to 2016 and as a Quality Engineer at bioMerieux from 2016 to 2017. His roles have involved various aspects of quality assurance and compliance within the healthcare sector.
Educational Background and Qualifications
Mahmoud Alsharbini earned a Bachelor of Science degree in Bioengineering from the University of Illinois at Chicago, completing his studies from 2005 to 2010. He furthered his education by obtaining a Master’s Degree in Business Administration and Management with a focus on Project Management from Keller Graduate School of Management of DeVry University, which he completed between 2016 and 2018.
Diverse Roles in Healthcare and Medical Device Industries
Throughout his career, Mahmoud has held various positions in the healthcare and medical device industries. His roles have included Verification & Validation Engineer at Hospira, Senior Engineer at Baxter International Inc., and Lab Technician at JointechLabs, Inc. This diverse experience has equipped him with a strong foundation in healthcare quality and research and development.
Expertise in EU Medical Device Regulation Compliance
Mahmoud possesses specialized expertise in EU Medical Device Regulation (MDR) compliance. This knowledge is essential for ensuring that medical devices meet regulatory standards in the European market, reflecting his commitment to quality and safety in healthcare products.